| scholarly article | Q13442814 |
| P50 | author | Valeriy Lukyanenko | Q56677226 |
| Robert J Bloch | Q87389477 | ||
| P2093 | author name string | Joaquin M Muriel | |
| P2860 | cites work | Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle | Q24308714 |
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| Dysferlin expression in tubular aggregates: their possible relationship to endoplasmic reticulum stress | Q28187229 | ||
| Defective membrane repair in dysferlin-deficient muscular dystrophy | Q28203095 | ||
| Caveolin regulates endocytosis of the muscle repair protein, dysferlin | Q28261848 | ||
| Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy | Q28281738 | ||
| Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle | Q28508989 | ||
| Membrane wounding triggers ATP release and dysferlin-mediated intercellular calcium signaling | Q28752070 | ||
| Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion. | Q30582564 | ||
| Rapid actin-cytoskeleton-dependent recruitment of plasma membrane-derived dysferlin at wounds is critical for muscle membrane repair | Q30583899 | ||
| An actin-dependent annexin complex mediates plasma membrane repair in muscle | Q30774985 | ||
| The endomembrane requirement for cell surface repair | Q30910745 | ||
| Dysferlin and the plasma membrane repair in muscular dystrophy | Q33201061 | ||
| Extensive mononuclear infiltration and myogenesis characterize recovery of dysferlin-null skeletal muscle from contraction-induced injuries | Q33655550 | ||
| Functional expression of transgenic 1sDHPR channels in adult mammalian skeletal muscle fibres | Q33801924 | ||
| The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: role of endogenous TLR ligands. | Q33808490 | ||
| Inflammasome up-regulation and activation in dysferlin-deficient skeletal muscle | Q33882512 | ||
| Ryanodine receptors: structure, expression, molecular details, and function in calcium release. | Q34024377 | ||
| Sustained overexpression of IGF-1 prevents age-dependent decrease in charge movement and intracellular Ca(2+) in mouse skeletal muscle | Q34177371 | ||
| Differential effects of voltage-dependent inactivation and local anesthetics on kinetic phases of Ca2+ release in frog skeletal muscle | Q34181894 | ||
| Distinct effects on Ca2+ handling caused by malignant hyperthermia and central core disease mutations in RyR1. | Q34187680 | ||
| Caspase-12 ablation preserves muscle function in the mdx mouse. | Q34211790 | ||
| Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repair. | Q34504075 | ||
| CD4+ cells, macrophages, MHC-I and C5b-9 involve the pathogenesis of dysferlinopathy | Q35632288 | ||
| The couplonopathies: A comparative approach to a class of diseases of skeletal and cardiac muscle. | Q35642611 | ||
| Myofiber damage precedes macrophage infiltration after in vivo injury in dysferlin-deficient A/J mouse skeletal muscle | Q35669024 | ||
| Unmasking potential intracellular roles for dysferlin through improved immunolabeling methods | Q35681845 | ||
| Skeletal and cardiac ryanodine receptors exhibit different responses to Ca2+ overload and luminal ca2+. | Q35696551 | ||
| Lysosome fusion to the cell membrane is mediated by the dysferlin C2A domain in coronary arterial endothelial cells | Q35883894 | ||
| Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B. | Q36482213 | ||
| Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B. | Q36677328 | ||
| Dysferlin in membrane trafficking and patch repair. | Q36839858 | ||
| Ryanodine receptor oxidation causes intracellular calcium leak and muscle weakness in aging. | Q36949333 | ||
| Impaired recovery of dysferlin-null skeletal muscle after contraction-induced injury in vivo | Q37143811 | ||
| DHPR activation underlies SR Ca2+ release induced by osmotic stress in isolated rat skeletal muscle fibers | Q37267643 | ||
| Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane | Q37409431 | ||
| Genetic manipulation of dysferlin expression in skeletal muscle: novel insights into muscular dystrophy | Q37413634 | ||
| Calcium-induced calcium release in skeletal muscle | Q37605472 | ||
| Dysferlin is essential for endocytosis in the sea star oocyte | Q37695556 | ||
| Pharmacology of transient receptor potential melastatin channels in the vasculature | Q37710139 | ||
| Dysferlin-deficient muscular dystrophy and innate immune activation. | Q38092854 | ||
| Genetic basis of limb-girdle muscular dystrophies: the 2014 update | Q38213016 | ||
| Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies | Q38918324 | ||
| Functional and pharmacological properties of human and rat NaV1.8 channels. | Q39860260 | ||
| Thrombospondin-1 levels correlate with macrophage activity and disease progression in dysferlin deficient mice | Q39959106 | ||
| Reduced threshold for luminal Ca2+ activation of RyR1 underlies a causal mechanism of porcine malignant hyperthermia | Q39978369 | ||
| Leaky ryanodine receptors delay the activation of store overload-induced Ca2+ release, a mechanism underlying malignant hyperthermia-like events in dystrophic muscle | Q40120301 | ||
| Elevated resting [Ca(2+)](i) in myotubes expressing malignant hyperthermia RyR1 cDNAs is partially restored by modulation of passive calcium leak from the SR. | Q40191570 | ||
| Measurement of resting cytosolic Ca2+ concentrations and Ca2+ store size in HEK-293 cells transfected with malignant hyperthermia or central core disease mutant Ca2+ release channels. | Q40984666 | ||
| Analysis of the dihydropyridine receptor site of L-type calcium channels by alanine-scanning mutagenesis | Q41098698 | ||
| Leaky ryanodine receptors in β-sarcoglycan deficient mice: a potential common defect in muscular dystrophy. | Q42149020 | ||
| In vivo Ca2+ dynamics induced by Ca2+ injection in individual rat skeletal muscle fibers | Q42316489 | ||
| Increased leakage of calcium ion from the sarcoplasmic reticulum of the mdx mouse | Q44688436 | ||
| Effects of low calcium and calcium antagonists on skeletal muscle staircase and fatigue | Q44967711 | ||
| The effect of the benzothiazepine diltiazem on force and Ca2+ current in isolated frog skeletal muscle fibres | Q45006350 | ||
| Diltiazem inhibits hKv1.5 and Kv4.3 currents at therapeutic concentrations | Q45146695 | ||
| Novel DYSF mutations in Thai patients with distal myopathy. | Q45984154 | ||
| Ca2+-dependent proteolysis of junctophilin-1 and junctophilin-2 in skeletal and cardiac muscle | Q46308630 | ||
| Target size analysis of skeletal muscle Ca2+ channels. Positive allosteric heterotropic regulation by d-cis-diltiazem is associated with apparent channel oligomer dissociation. | Q47252918 | ||
| Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology | Q47966217 | ||
| Transfer of high sensitivity for benzothiazepines from L-type to class A (BI) calcium channels | Q48975234 | ||
| Transfer of L-type calcium channel IVS6 segment increases phenylalkylamine sensitivity of alpha1A. | Q49010921 | ||
| Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency | Q50489087 | ||
| Quantitative evaluation of mammalian skeletal muscle as a heterologous protein expression system. | Q50746364 | ||
| Fundamental properties of local anesthetics: half-maximal blocking concentrations for tonic block of Na+ and K+ channels in peripheral nerve. | Q51498752 | ||
| Respiratory and cardiac function in japanese patients with dysferlinopathy. | Q51620573 | ||
| Components of charge movement in rabbit skeletal muscle: the effect of tetracaine and nifedipine. | Q51806334 | ||
| The sodium channel from rat brain. Reconstitution of neurotoxin-activated ion flux and scorpion toxin binding from purified components. | Q51848153 | ||
| Effect of tetracaine on veratrine-mediated influx of sodium into rat brain synaptosomes. | Q51854420 | ||
| Calpains, cleaved mini-dysferlinC72, and L-type channels underpin calcium-dependent muscle membrane repair. | Q53115389 | ||
| The distribution and characterization of skeletal muscle lesions in dysferlin-deficient SJL and A/J mice. | Q53382916 | ||
| Local calcium release in mammalian skeletal muscle. | Q53945064 | ||
| Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model. | Q54520022 | ||
| Identification of putative calcium channels in skeletal muscle microsomes. | Q55062469 | ||
| Slow inward calcium currents have no obvious role in muscle excitation–contraction coupling | Q59077487 | ||
| Molecular determinants of high affinity phenylalkylamine block of L-type calcium channels in transmembrane segment IIIS6 and the pore region of the alpha1 subunit. | Q64980401 | ||
| Effect of calcium antagonist drugs on calcium currents in mammalian skeletal muscle fibers | Q68953031 | ||
| Molecular determinants of diltiazem block in domains IIIS6 and IVS6 of L-type Ca(2+) channels | Q73229753 | ||
| Ca2+ sparks and Ca2+ waves in saponin-permeabilized rat ventricular myocytes | Q73280404 | ||
| Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation | Q73680942 | ||
| Dantrolene inhibition of sarcoplasmic reticulum Ca2+ release by direct and specific action at skeletal muscle ryanodine receptors | Q73813668 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 17 | |
| P304 | page(s) | 5191-5207 | |
| P577 | publication date | 2017-06-26 | |
| P1433 | published in | Journal of Physiology | Q7743612 |
| P1476 | title | Coupling of excitation to Ca2+ release is modulated by dysferlin | |
| P478 | volume | 595 |
| Q64061047 | Dysferlin-deficiency has greater impact on function of slow muscles, compared with fast, in aged BLAJ mice |
| Q92826260 | Ferlin Overview: From Membrane to Cancer Biology |
| Q89921518 | Functions of Vertebrate Ferlins |
| Q49689341 | New Insights in Cardiac Calcium Handling and Excitation-Contraction Coupling. |
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